A Semi-Markov Model for Mitosis Segmentation in Time-Lapse Phase Contrast Microscopy Image Sequences of Stem Cell Populations

被引:61
作者
Liu, An-An [1 ]
Li, Kang [2 ]
Kanade, Takeo [3 ]
机构
[1] Tianjin Univ, Sch Elect Informat Engn, Tianjin 300072, Peoples R China
[2] Microsoft Corp, Redmond, WA 98052 USA
[3] Carnegie Mellon Univ, Inst Robot, Pittsburgh, PA 15213 USA
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
Hidden conditional random fields; large-scale cell population; mitosis detection; phase contrast microscopy; sequence segmentation; semi-Markov model; LINEAGE CONSTRUCTION; TRACKING;
D O I
10.1109/TMI.2011.2169495
中图分类号
TP39 [计算机的应用];
学科分类号
081203 ; 0835 ;
摘要
We propose a semi-Markov model trained in a max-margin learning framework for mitosis event segmentation in large-scale time-lapse phase contrast microscopy image sequences of stem cell populations. Our method consists of three steps. First, we apply a constrained optimization based microscopy image segmentation method that exploits phase contrast optics to extract candidate subsequences in the input image sequence that contains mitosis events. Then, we apply a max-margin hidden conditional random field (MM-HCRF) classifier learned from human-annotated mitotic and nonmitotic sequences to classify each candidate subsequence as a mitosis or not. Finally, a max-margin semi-Markov model (MM-SMM) trained on manually-segmented mitotic sequences is utilized to reinforce the mitosis classification results, and to further segment each mitosis into four predefined temporal stages. The proposed method outperforms the event-detection CRF model recently reported by Huh et al. as well as several other competing methods in very challenging image sequences of multipolar-shaped C3H10T1/2 mesenchymal stem cells. For mitosis detection, an overall precision of 95.8% and a recall of 88.1% were achieved. For mitosis segmentation, the mean and standard deviation for the localization errors of the start and end points of all mitosis stages were well below 1 and 2 frames, respectively. In particular, an overall temporal location error of 0.73 +/- 1.29 frames was achieved for locating daughter cell birth events.
引用
收藏
页码:359 / 369
页数:11
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